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Merck
모든 사진(3)

주요 문서

140023

Sigma-Aldrich

Tetraethylammonium bromide

reagent grade, 98%

동의어(들):

TEAB, TEA bromide

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About This Item

Linear Formula:
(C2H5)4N(Br)
CAS Number:
Molecular Weight:
210.16
Beilstein:
3563430
EC Number:
MDL number:
UNSPSC 코드:
12352107
PubChem Substance ID:
NACRES:
NA.22

Grade

reagent grade

Quality Level

분석

98%

형태

crystalline

불순물

≤2% triethylamine hydrobromide

pH

6.5 (100 g/L)

mp

285 °C (dec.) (lit.)

SMILES string

[Br-].CC[N+](CC)(CC)CC

InChI

1S/C8H20N.BrH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1

InChI key

HWCKGOZZJDHMNC-UHFFFAOYSA-M

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관련 카테고리

애플리케이션

Tetraethylammonium bromide may be used:
  • As an organic template for synthesizing zeolite beta via hydrothermal crystallization.
  • As a catalyst for the oxidative coupling of aldehydes or alcohols with thiophenols or disulfides to form thioesters.
  • In combination with o-iodoxybenzoic acid (IBX) for the oxidative dehomologation of primary carboxamides to nitriles and α,α-disubstituted acetamides to ketones. This reagent combination can also be used for the conversion of sulfides to sulfoxides and N,N-disubstituted glycylamides into corresponding cyanamides.

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

361.4 °F - closed cup

Flash Point (°C)

183 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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이미 열람한 고객

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1 of 1

Novel and facile transformation of N, N-disubstituted glycylamides into corresponding cyanamides by using pentavalent iodine reagents in combination with tetraethylammonium bromide.
Chaudhari K
Synlett, 18, 2815-2818 (2007)
Oxidative Conversion of ?, ?-Disubstituted Acetamides to Corresponding One-Carbon-Shorter Ketones Using Hypervalent Iodine (?5) Reagents in Combination with Tetraethylammonium Bromide.
Bellale E
The Journal of Organic Chemistry, 73(23), 9473-9475 (2008)
Hydrothermal crystallization of zeolite beta using tetraethylammonium bromide.
Eapen M
Zeolites, 14(4), 295-302 (1994)
A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst.
Shukla V
The Journal of Organic Chemistry, 68(13), 5422-5425 (2003)
Tetraethylammonium Bromide?Catalyzed Oxidative Thioesterification of Aldehydes and Alcohols.
Zhu X
Advanced Synthesis & Catalysis, 355(18), 3558-3562 (2013)

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